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Journal Abstract Search

146 related items for PubMed ID: 32413569

  • 21. Clinically Different Presentations of Family Members With the Same Homozygote Diacylglycerol Kinase Epsilon Mutation: Case Report.
    Çelikkaya E, Güngör T, Karakaya D, Kargın Çakıcı E, Yazılıtaş F, Özaltın F, Bülbül M.
    Exp Clin Transplant; 2022 May; 20(Suppl 3):45-48. PubMed ID: 35570599
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  • 22. [Genetic analysis of a child with atypical Hemolytic uremic syndrome and nephrotic-range proteinuria].
    Wang D, Shan C, Gao T, Liu J, Zhang R, Zhang Q, Chang H, Lin Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Dec 10; 40(12):1560-1565. PubMed ID: 37994143
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  • 23. Mutation spectrum of genes associated with steroid-resistant nephrotic syndrome in Chinese children.
    Wang Y, Dang X, He Q, Zhen Y, He X, Yi Z, Zhu K.
    Gene; 2017 Aug 20; 625():15-20. PubMed ID: 28476686
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  • 24. Simultaneous sequencing of 24 genes associated with steroid-resistant nephrotic syndrome.
    McCarthy HJ, Bierzynska A, Wherlock M, Ognjanovic M, Kerecuk L, Hegde S, Feather S, Gilbert RD, Krischock L, Jones C, Sinha MD, Webb NJ, Christian M, Williams MM, Marks S, Koziell A, Welsh GI, Saleem MA, RADAR the UK SRNS Study Group.
    Clin J Am Soc Nephrol; 2013 Apr 20; 8(4):637-48. PubMed ID: 23349334
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  • 25. Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children.
    Dhandapani MC, Venkatesan V, Rengaswamy NB, Gowrishankar K, Ekambaram S, Sengutavan P, Perumal V.
    Clin Exp Nephrol; 2017 Feb 20; 21(1):127-133. PubMed ID: 26820844
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  • 26. Rapid recovery of membrane cofactor protein (MCP; CD46) associated atypical haemolytic uraemic syndrome with plasma exchange.
    Reid VL, Mullan A, Erwig LP.
    BMJ Case Rep; 2013 Sep 04; 2013():. PubMed ID: 24005975
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  • 31. NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.
    Weber S, Gribouval O, Esquivel EL, Morinière V, Tête MJ, Legendre C, Niaudet P, Antignac C.
    Kidney Int; 2004 Aug 04; 66(2):571-9. PubMed ID: 15253708
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  • 33. A Systematic Analysis of Major Susceptible Genes in Childhood-onset Steroid-resistant Nephrotic Syndrome.
    Li Y, He Q, Wang Y, Dang X, Wu X, Li X, Shuai L, Yi Z.
    Ann Clin Lab Sci; 2019 May 04; 49(3):330-337. PubMed ID: 31308032
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  • 34. Haemolytic uraemic syndrome.
    Fakhouri F, Zuber J, Frémeaux-Bacchi V, Loirat C.
    Lancet; 2017 Aug 12; 390(10095):681-696. PubMed ID: 28242109
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  • 36. [Atypical hemolytic-uremic syndrome related to abnormalities within the complement system].
    Frémeaux-Bacchi V, Fakhouri F, Roumenina L, Dragon-Durey MA, Loirat C.
    Rev Med Interne; 2011 Apr 12; 32(4):232-40. PubMed ID: 21376430
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